Canonical Allele Identifier: CA389413437

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269508G>C (hg19) ; chr14:g.33800302G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800302G>C , CM000676.2:g.33800302G>C	GRCh38
NC_000014.8:g.34269508G>C , CM000676.1:g.34269508G>C	GRCh37
NC_000014.7:g.33339259G>C	NCBI36
NG_013036.1:g.866050G>C
NG_013036.2:g.866050G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1995G>C MANE Select	ENSP00000348460.4:p.Trp665Cys
ENST00000551634.6:c.2004G>C	ENSP00000448373.2:p.Trp668Cys
ENST00000680362.1:c.1895G>C
ENST00000681323.1:c.793+2721G>C
ENST00000346562.6:c.1899G>C	ENSP00000319610.5:p.Trp633Cys
ENST00000356141.8:c.1995G>C	ENSP00000348460.4:p.Trp665Cys
ENST00000357798.9:c.1956G>C	ENSP00000350446.5:p.Trp652Cys
ENST00000548645.5:c.1905G>C	ENSP00000448916.1:p.Trp635Cys
ENST00000551492.5:c.2010G>C	ENSP00000450392.1:p.Trp670Cys
ENST00000551634.5:c.1917G>C	ENSP00000448373.1:p.Trp639Cys
NM_001164749.1:c.1995G>C	NP_001158221.1:p.Trp665Cys
NM_001165893.1:c.1905G>C	NP_001159365.1:p.Trp635Cys
NM_022123.2:c.1899G>C	NP_071406.1:p.Trp633Cys
NM_173159.2:c.1956G>C	NP_775182.1:p.Trp652Cys
XM_005267991.2:c.2016G>C	XP_005268048.1:p.Trp672Cys
XM_005267992.2:c.2010G>C	XP_005268049.1:p.Trp670Cys
XM_005267993.2:c.1956G>C	XP_005268050.1:p.Trp652Cys
XM_011537067.1:c.2046G>C	XP_011535369.1:p.Trp682Cys
XM_011537068.1:c.2037G>C	XP_011535370.1:p.Trp679Cys
XM_011537069.1:c.2007G>C	XP_011535371.1:p.Trp669Cys
XM_011537070.1:c.1950G>C	XP_011535372.1:p.Trp650Cys
XM_011537071.1:c.1917G>C	XP_011535373.1:p.Trp639Cys
XM_011537072.1:c.1896G>C	XP_011535374.1:p.Trp632Cys
XM_011537073.1:c.1689G>C	XP_011535375.1:p.Trp563Cys
XM_011537074.1:c.1689G>C	XP_011535376.1:p.Trp563Cys
XM_005267991.3:c.2103G>C	XP_005268048.2:p.Trp701Cys
XM_005267992.3:c.2097G>C	XP_005268049.2:p.Trp699Cys
XM_011537067.2:c.2046G>C	XP_011535369.1:p.Trp682Cys
XM_011537069.2:c.2094G>C	XP_011535371.2:p.Trp698Cys
XM_011537070.2:c.1950G>C	XP_011535372.1:p.Trp650Cys
XM_011537071.2:c.2004G>C	XP_011535373.2:p.Trp668Cys
XM_011537072.2:c.1896G>C	XP_011535374.1:p.Trp632Cys
XM_017021582.1:c.2154G>C	XP_016877071.1:p.Trp718Cys
XM_017021583.1:c.2145G>C	XP_016877072.1:p.Trp715Cys
XM_017021584.1:c.2064G>C	XP_016877073.1:p.Trp688Cys
XM_017021585.1:c.2013G>C	XP_016877074.1:p.Trp671Cys
XM_017021586.1:c.1689G>C	XP_016877075.1:p.Trp563Cys
XM_017021587.1:c.1689G>C	XP_016877076.1:p.Trp563Cys
XM_017021588.1:c.1689G>C	XP_016877077.1:p.Trp563Cys
NM_001164749.2:c.1995G>C MANE Select	NP_001158221.1:p.Trp665Cys
NM_001165893.2:c.1905G>C	NP_001159365.1:p.Trp635Cys
NM_022123.3:c.1899G>C	NP_071406.1:p.Trp633Cys
NM_173159.3:c.1956G>C	NP_775182.1:p.Trp652Cys
NM_001394988.1:c.1950G>C	NP_001381917.1:p.Trp650Cys
NM_001394989.1:c.1896G>C	NP_001381918.1:p.Trp632Cys